rs10494836
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10494836(C;C) |
| Make rs10494836(C;T) |
| Make rs10494836(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 202727750 |
| Gene | KDM5B |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10494836 |
| dbSNP (classic) | rs10494836 |
| ClinGen | rs10494836 |
| ebi | rs10494836 |
| HLI | rs10494836 |
| Exac | rs10494836 |
| Gnomad | rs10494836 |
| Varsome | rs10494836 |
| LitVar | rs10494836 |
| Map | rs10494836 |
| PheGenI | rs10494836 |
| Biobank | rs10494836 |
| 1000 genomes | rs10494836 |
| hgdp | rs10494836 |
| ensembl | rs10494836 |
| geneview | rs10494836 |
| scholar | rs10494836 |
| rs10494836 | |
| pharmgkb | rs10494836 |
| gwascentral | rs10494836 |
| openSNP | rs10494836 |
| 23andMe | rs10494836 |
| SNPshot | rs10494836 |
| SNPdbe | rs10494836 |
| MSV3d | rs10494836 |
| GWAS Ctlg | rs10494836 |
| GMAF | 0.1107 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 23188672] Genetic variation in a hsa-let-7 binding site in RAD52 is associated with breast cancer susceptibility
